BluB/CobT2 fusion enzyme activity reveals mechanisms responsible for production of active form of vitamin B 12 by Propionibacterium freudenreichii

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Deptula , P , Kylli , P T , Chamlagain , B S , Holm , L U T , Kostiainen , R K , Piironen , V I , Savijoki , K K & Varmanen , P K 2015 , ' BluB/CobT2 fusion enzyme activity reveals mechanisms responsible for production of active form of vitamin B 12 by Propionibacterium freudenreichii ' , Microbial Cell Factories , vol. 14 , 186 . https://doi.org/10.1186/s12934-015-0363-9

Title: BluB/CobT2 fusion enzyme activity reveals mechanisms responsible for production of active form of vitamin B 12 by Propionibacterium freudenreichii
Author: Deptula, Paulina; Kylli, Petri Tapio; Chamlagain, Bhawani Shankar; Holm, Liisa Ulrika Teodora; Kostiainen, Risto Kalervo; Piironen, Vieno Irene; Savijoki, Kirsi Kristiina; Varmanen, Pekka Kristian
Contributor organization: Department of Food and Nutrition
Molecular Dairy Microbiology
Food quality and safety: lipids, vitamins and other bioactive compounds
Faculty of Pharmacy
Division of Pharmaceutical Chemistry and Technology
Biosciences
Computational genomics
Genetics
Institute of Biotechnology
Risto Kostiainen / Principal Investigator
Bioinformatics
Drug Research Program
Food Sciences
Date: 2015-11-23
Language: eng
Number of pages: 12
Belongs to series: Microbial Cell Factories
ISSN: 1475-2859
DOI: https://doi.org/10.1186/s12934-015-0363-9
URI: http://hdl.handle.net/10138/182611
Abstract: Background Propionibacterium freudenreichii is a food grade bacterium that has gained attention as a producer of appreciable amounts of cobalamin, a cobamide with activity of vitamin B 12 . Production of active form of vitamin is a prerequisite for attempts to naturally fortify foods with B 12 by microbial fermentation. Active vitamin B 12 is distinguished from the pseudovitamin by the presence of 5,6-dimethylbenzimidazole (DMBI) as the lower ligand. Genomic data indicate that P. freudenreichii possesses a fusion gene, bluB/cobT2, coding for a predicted phosphoribosyltransferase/nitroreductase, which is presumably involved in production of vitamin B 12 . Understanding the mechanisms affecting the synthesis of different vitamin forms is useful for rational strain selection and essential for engineering of strains with improved B 12 production properties. Results Here, we investigated the activity of heterologously expressed and purified fusion enzyme BluB/CobT2. Our results show that BluB/CoBT2 is responsible for the biosynthesis of the DMBI base and its activation into α-ribazole phosphate, preparing it for attachment as the lower ligand of cobalamin. The fusion enzyme was found to be efficient in metabolite channeling and the enzymes’ inability to react with adenine, a lower ligand present in the pseudovitamin, revealed a mechanism favoring the production of the active form of the vitamin. P. freudenreichii did not produce cobalamin under strictly anaerobic conditions, confirming the requirement of oxygen for DMBI synthesis. In vivo experiments also revealed a clear preference for incorporating DMBI over adenine into cobamide under both microaerobic and anaerobic conditions. Conclusions The herein described BluB/CobT2 is responsible for the production and activation of DMBI. Fusing those two activities results in high pressure towards production of the true vitamin B 12 by efficiently activating DMBI formed within the same enzymatic complex. This indicates that BluB/CobT2 is the crucial enzyme in the B 12 biosynthetic pathway of P. freudenreichii. The GRAS organism status and the preference for synthesizing active vitamin form make P. freudenreichii a unique candidate for the in situ production of vitamin B 12 within food products. Keywords: Propionibacterium freudenreichii ; Cobalamin; B12; DMBI; α-Ribazole; Phosphoribozyltransferase; Nitroreductase; Fusion enzyme; BluB; CobT
Subject: 1182 Biochemistry, cell and molecular biology
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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